Petrels are among the most threatened group of birds. On top of facing predation by introduced mammals and incidental bycatch, these seabirds have to deal with an emerging threat, light pollution, which is increasing globally. Fledglings are disorientated and attracted to artificial lights in their maiden night flights from their nests to the sea. Once grounded, they are exposed to multiple threats leading to high mortality. We report on numbers of three petrel species (Balearic shearwater Puffinus mauretanicus, Scopoli's shearwater Calonectris diomedea, and European storm-petrel Hydrobates pelagicus) rescued on the Balearic Islands, Mediterranean Sea, in the period 1999-2013. We assessed the proportion of grounded fledglings in the population and colonies impact based on radiance levels measured from a nocturnal satellite image. We also calculated the radius of light pollution impact. At least 304 fledgling birds were found stranded due to attraction to artificial lights, 8.5% of them being fatally affected. Proportion of grounded fledglings ranged between 0.13-0.56% of the fledglings produced annually. The body mass of Balearic and Scopoli's shearwater fledglings decreased with rescue date. Light-induced mortality increased during fledging period for Scopoli's shearwaters. Birds were rescued at a mean distance of 4,833 m from the nearest colony and between 30-47% of colonies were exposed to light-polluted areas. Although impact seems to be low for all species, urban development and, consequently, the increase in light pollution in the proximities of the colonies should be taken into account to reduce as much as possible this emerging source of mortality.
Traumatic peripheral nerve neurotmesis occurs frequently and functional recovery is often slow and impaired. Induced pluripotent stem cells (iPSCs) have shown much promise in recent years due to its regenerative properties similar to that of embryonic stem cells. However, the potential of iPSCs in promoting the functional recovery of a transected peripheral nerve is largely unknown. This study is the first to investigate in vivo effects of episomal iPSCs (EiPSCs) on peripheral nerve regeneration in a murine sciatic nerve transection model. Episomal iPSCs refer to iPSCs that are generated via Oct3/4-Klf4-Sox2 plasmid reprogramming instead of the conventional viral insertion techniques. It represents a relatively safer form of iPSC production without permanent transgene integration which may raise questions regarding risks of genomic mutation. A minimal number of EiPSCs were added directly to the transected nerve. Functional recovery of the EiPSC group was significantly improved compared to the negative control group when assessed via serial five-toe spread measurement and gait analysis of ankle angles. EiPSC promotion of nerve regeneration was also evident on stereographic analysis of axon density, myelin thickness, and axonal cross-sectional surface area. Most importantly, the results observed in EiPSCs are similar to that of the embryonic stem cell group. A roughly ten-fold increase in neurotrophin-3 levels was seen in EiPSCs which could have contributed to peripheral nerve regeneration and recovery. No abnormal masses or adverse effects were noted with EiPSC administration after one year of follow-up. We have hence shown that functional recovery of the transected peripheral nerve can be improved with the use of EiPSC therapy, which holds promise for the future of nerve regeneration.
Background: In immunologic research, mice have advantages over other animals, such as low costs, easy handling, suitable life cycle, and adequate laboratory resources. However, vascularized composite allotransplantation surgery using mice is not popular, partly because of technical difficulties and high mortality rates. The authors’ goal was to demonstrate a face transplantation model in mice that includes skin, mandible, and oral mucosa. Methods: The authors developed a new syngeneic face transplantation model composed of skin, mandible, teeth, and oral mucosa in C57BL/6 mice. The following assessment included measuring the length of the right incisor on the transplanted mandibles, computed tomographic scan in one mouse for mandibular structure evaluation, and histologic examination of different tissue samples in another mouse for viability evaluation. Results: The authors performed five consecutive transplantations. The donor vessels were the common carotid artery (approximately equal to 0.4 mm) and the anterior facial vein (approximately equal to 0.2 mm), and the recipients were the common carotid artery and the posterior facial vein (approximately equal to 0.4 mm). The mean operative time was 80 minutes for the donor and 123 minutes for the recipient. There were neither flap failures nor animal deaths. The follow-up was 6 months. The right incisor of the transplant grew at different rates in all cases. Histologic samples showed viability in all tissues, including mandibular bone marrow. Computed tomography demonstrated normal structure of the transplanted bone. Conclusion: The authors’ syngeneic partial face transplantation model in mice, which included skin, oral mucosa, and mandible with teeth, should be useful for future face allotransplantation research, as the myriad of tissues it provides, of different immunomodulatory functions, is similar to that in the clinical scenario.
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